A strained vicinal diol as a reductant for coupling of organyl halides
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DOI[10.1246/cl.190403]to the data of the same series
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- Material Type
- 記事
- Author/Editor
- Naoki IshidaYusuke MasudaFangzhu Sun
- Publication, Distribution, etc.
- Publication Date
- 2019-06-06
- Publication Date (W3CDTF)
- 2019-06-06
- Periodical title
- Chemistry letters
- No. or year of volume/issue
- 48(9)
- Volume
- 48(9)
- ISSN (Periodical Title)
- 1348-0715
- ISSN-L (Periodical Title)
- 0366-7022
- Text Language Code
- eng
- DOI
- 10.1246/cl.190403
- Persistent ID (NDL)
- info:ndljp/pid/11552465
- Collection
- Collection (Materials For Handicapped People:1)
- Collection (particular)
- 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
- Acquisition Basis
- オンライン資料収集制度
- Date Accepted (W3CDTF)
- 2020-10-07T08:55:27+09:00
- Date Captured (W3CDTF)
- 2019-08-21
- Format (IMT)
- application/pdf
- Access Restrictions
- 国立国会図書館内限定公開
- Service for the Digitized Contents Transmission Service
- 図書館・個人送信対象外
- Availability of remote photoduplication service
- 可
- Periodical Title (URI)
- Periodical Title (Persistent ID (NDL))
- info:ndljp/pid/11552460
- Data Provider (Database)
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- Summary, etc.
- コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
- DOI
- 10.1246/cl.190403
- Access Restrictions
- インターネット公開
- Related Material (URI)
- Is Referenced By
- Thermal Metathesis of C–C Single Bonds Induced by Steric Frustration
- References
- Reductive Cross‐Coupling Reactions between Two ElectrophilesMechanism and Selectivity in Nickel-Catalyzed Cross-Electrophile Coupling of Aryl Halides with Alkyl HalidesSalt‐Free Reduction of Nonprecious Transition‐Metal Compounds: Generation of Amorphous Ni Nanoparticles for Catalytic C–C Bond FormationAryl Ketones as Single‐Electron‐Transfer Photoredox Catalysts in the Nickel‐Catalyzed Homocoupling of Aryl HalidesPreparation of Ni(cod)<sub>2</sub> Using Light as the Source of EnergyComplexation with diol host compounds. Part 2. Structures of 1,1,2,2-tetraphenylethane-1,2-diol and its 1?2 molecular inclusion complex with dimethylsulphoxideNickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Alkyl HalidesReactivity of ketyl free radicals. Part 2.—Dimerization and dismutation of fluorenone and xanthone ketylsBimetallic C–C Bond-Forming Reductive Elimination from Nickel1,2-Ethanediol (Ethylene Glycol) at 130KCrystalline ethane-1,2-diol does not have intra-molecular hydrogen bonding: Experimental and theoretical charge density studiesReaction of .pi.-allylnickel bromide complexes with organic halides. Stereochemistry and mechanismElectronic Interaction in Ketyl RadicalsNickel‐Catalyzed Cross‐Electrophile Coupling with Organic Reductants in Non‐Amide SolventsSynthesis with zerovalent nickel. Coupling of aryl halides with bis(1,5-cyclooctadiene)nickel(0)Coupling of aryl chlorides by nickel and reducing metalsgeneration of a solvated zerovalent nickel reagent. Biaryl formation2,3-Dimethyl-2,3-butanediol (pinacol)Nickel-phosphine complex-catalyzed homo coupling of aryl halides in the presence of zinc powderStructures and vibrational spectra of pinacol. Part 2. A new crystal form of pinacol: a key to the infrared spectroscopic identification of the G and T conformers in condensed phasesPalladium-Catalyzed Tetrakis(dimethylamino)ethylene-Promoted Reductive Coupling of Aryl HalidesNickel-catalyzed reductive coupling of alkyl halides with other electrophiles: concept and mechanistic considerationsMethods and Mechanisms for Cross-Electrophile Coupling of Csp<sup>2</sup> Halides with Alkyl ElectrophilesMechanism of CC coupling reactions of aromatic halides, promoted by Ni(COD)2 in the presence of 2,2′-bipyridine and PPh3, to give biarylsMechanism of biaryl synthesis with nickel complexesBENZOPINACOLAryl−Aryl Bond Formation One Century after the Discovery of the Ullmann ReactionFirst Isolation of a Metal Ketyl in Aggregated Forms. X-ray Structures of Dimeric and Tetrameric Sodium Fluorenone Ketyl Complexes: [Na(μ<sub>2</sub>-η<sup>1</sup>-ketyl)(HMPA)<sub>2</sub>]<sub>2</sub> and [Na(μ<sub>3</sub>-η<sup>1</sup>-ketyl)(HMPA)]<sub>4</sub>Lithium Hydride Mediated Nickel(0) Catalysed Biaryl Synthesis from Aryl Chlorides and Bromides.sigma.-Aryl compounds of nickel, palladium, and platinum. Synthesis and bonding studiesNickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Alkyl Bromides: Et<sub>3</sub>N as the Terminal Reductant
- Data Provider (Database)
- 国立情報学研究所 : CiNii Research
- Original Data Provider (Database)
- 雑誌記事索引データベースCrossrefCiNii Articles科学研究費助成事業データベース科学研究費助成事業データベース科学研究費助成事業データベースCrossref
- Bibliographic ID (NDL)
- 11552465
- NAID
- 130007703046